# Research Nurse > NHS job listing from Job Clerk for Liverpool University Hospitals NHS Foundation Trust. ## Canonical URLs - **HTML:** https://www.jobclerk.com/job/research-nurse/6bcf882c-36ee-4989-beba-31208af01ad1 - **Markdown:** https://www.jobclerk.com/job/research-nurse/6bcf882c-36ee-4989-beba-31208af01ad1.md ## Summary - **Status:** Live - **Employer:** Liverpool University Hospitals NHS Foundation Trust - **Location:** Royal Liverpool University Hospital - **Workplace type:** onsite - **Profession:** Research nurse - **Grade:** Band 6 - **Salary:** £39,959 - £48,117 per annum - **Contract type:** Permanent - **Employment type:** Full time - 37.5 hours per week - **Closing date:** 2026-10-30T23:59:00.000Z - **Posted:** 2026-10-16T12:55:02.738Z - **Source information URL:** https://www.healthjobsuk.com/job/UK/Merseyside/Liverpool/Liverpool_University_Hospitals_NHS_Foundation_Trust/clinical_research/clinical_research-v8335623 - **Application URL:** https://apps.trac.jobs/job-advert/8335623?ShowJobAdvert=&feedid=9002 - **Employer website:** https://www.liverpoolft.nhs.uk ## Job Content ### Job overview The Liverpool University Hospitals NHS Foundation Trust has an exciting developmental opportunity for a band 6 clinical research nurse post in rheumatology/MSK. The successful candidate will be responsible for the day-to-day running of research studies, including patient screening, recruitment, informed consent processes, and data management. The position requires excellent communication and interpersonal skills, as well as the ability to work independently and meet tight deadlines. The primary base for the post is Aintree University Hospital. ### Main duties of the job To contribute to all aspects of the planning, conduct and reporting of all clinical trials within the research speciality To be responsible for the day-to-day management of, patient recruitment to research studies To work on a daily basis with minimal supervision as part of a research team To ensure that all clinical research activity is ICH GCP compliant and conducted in accordance with the agreed protocols. To maintain a high standard of patient care in line with Trust and R&D policies and protocols and in accordance with the Research Governance Framework. To ensure that all data is collected and managed effectively and accurately To contribute to all aspects of the planning, conduct and reporting of all clinical trials within the research speciality Knowledge of clinical research including issues on ethics, law, drug development and management in clinical issues Partly responsible for submissions to research ethics committees Maintaining overall standard of care for patients at all times Educational and developmental role Ability to give advice on the organisation and management of research in progress Liaison with sponsor companies and multi-disciplinary research teams ### Detailed job description and main responsibilities To assist the clinicians in the assessment of patients/volunteers for eligibility for research and monitoring of their condition throughout their participation. To provide ongoing advice and information to patients/volunteers with regard to their participation in clinical research in order to facilitate effective informed consent. To assist the clinicians to report and record any adverse events as dictated by Trust and Departmental protocols. To assist the clinicians with protocol development and ethical approval. To assist in the analysis of data and preparation of reports for presentation and publication. To co-ordinate and carry out patient visits in accordance with study protocols, including co-ordinating special tests in other departments, collection of data, coding, data entry and patient support To carry out treatment procedures and treatment interventions according to predetermined protocols, including venepuncture, venous cannulation, administering of intra-venous drugs and vital sign recording To report on a regular basis to the Senior Nurse of the R&D department for professional support and guidance. To ensure that all clinical research activity is ICH GCP compliant and conducted in accordance with the agreed protocols To maintain a high standard of patient care in line with Trust and R&D policies and protocols and in accordance with the Research Governance Framework To ensure that all data is collected and managed accurately To carry out the collection, processing and shipping of biological specimens according to protocol requirements and follow up appropriately on alert values To be involved in the education of patients and their various aspects of their disease To ensure that patient safety is paramount in all procedures that take place for trial purposes To ensure clinical and research documentation and record keeping is completed accurately and efficiently in accordance with the EU Directive, ICH GCP Guidelines. To work within the N.M.C Code Of Conduct and scope of professional conduct To have sufficient computer skills for the handling and management of computerised data To keep up to date with relevant medical literature, developments in clinical research methodology, monitoring and local regulatory and ethical requirements To attend research network meetings, attend courses, conferences and study days in order to remain up to date with all relevant aspects of clinical research To participate in the education and development of staff/students, e.g. clinical supervision and ensure that all personnel are adequately informed about, and comply with all details of the trials. To participate in the education and development of student nurses. The post holder will be expected to work clinical shifts in a ward environment if necessary ### Applicant requirements You must have appropriate UK professional registration. This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service. ## Person Specification ### other **Essential** - Possession of tact and sensitivity to the needs of both patients and colleagues, including a commitment to confidentiality - Meticulous attention to detail and a high standard of accuracy - Flexible approach to working hours ### Skills **Essential** - Ability to use a personal computer, (computer literacy and proficiency in MS Office / EDCL) - Skills in administration and project management - Good communication, presentational, training and interpersonal skills - Ability to meet tight deadlines and cope in a highly demanding environment - Ability to work independently and prioritise / own workload and to communicate effectively with all members of the multi-disciplinary team - Excellent and effective verbal and written communication skills **Desirable** - Skills in handling and management of computerised data - Skills required to evaluate and assist in developing new protocols - Skills in the analysis and interpretation of data ### Knowledge **Essential** - Knowledge of the principles and practice of clinical research and/or clinical trials - Understanding of the role & responsibilities of a Clinical Research Nurse - Knowledge of ethical and quality standards applicable to clinical trials, including EU Directive on ICH GCP requirements **Desirable** - Knowledge of the Health Service, R&D, the pharmaceutical industry partnership and relevant information sciences ### Experience **Essential** - Demonstrable experience of patient education and counselling, e.g. providing lifestyle advice - Clinical experience/qualification in venepuncture, IV cannulation - Supervision of student nurses - Previous experience of co-ordinating clinical research studies - Experience of liaison with staff at all levels in Healthcare **Desirable** - Previous experience within the research speciality - Appraisal and interviewing skills ### Qualifications **Essential** - RGN - Current NMC registration - Attendance of recent short courses and/or study days on research **Desirable** - 1st level degree or studying towards - Research Qualifications ## Documents - [band 6 research nurse (pdf, 154.7kb)](https://www.healthjobsuk.com/documents?vdoc=10659309) - [life at luhft benefits (pdf, 333.2kb)](https://www.healthjobsuk.com/documents?edoc=2664) - [research nurse risk id (pdf, 184.7kb)](https://www.healthjobsuk.com/documents?vdoc=10659310) - [research nurse advert rheumatology (pdf, 72.4kb)](https://www.healthjobsuk.com/documents?vdoc=10659311) ## Agent Notes - This Markdown page is generated from the same Job Clerk job record as the HTML job detail page. - Use the canonical HTML URL for user-facing references. - Use the application URL when the user wants to apply on the source NHS site.